Are you interested in selling your medical device in various countries, but are not sure how to go about meeting the Medical Device Regulatory requirements or quality standards
Maven offers you a yearly programs (standard / customised) to maintain your Regulatory requirements without any hassle.
Commercializing your medical device first requires you to obtain registration and approval from regulatory agencies in each country where you plan to place devices on the market.
A quality management system is a collection of business processes focused on consistently meeting customer requirements and enhancing their satisfaction. It is aligned with an organization's purpose and strategic direction.
It is easy to make mistakes in the regulatory process that can delay market entry or incur unnecessary costs.
Our medical devices courses allow you to have a detailed look at some of the most important sections of bringing a successful product to market within this highly regulated sector.
Maven is a medical device consulting company which provides regulatory guidance to various manufacturers in the healthcare industry to ensure the strategic development of these manufacturers.
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Maven Profcon Services LLP is a service provider for Consultation, Audits, Trainings, GAP audits, Conformity Assessments, Various Evaluation, Documents Review & Testing. Supported with the team of Management Graduates, Engineering Graduates, Technical experts, Subject experts, Trainers and lead auditors.
Our services are in diversified dimensions to cater manufacturing and service organizations.Organization has Association with some of the top professionals for sharing of technical expertise in different area. These individuals have revolutionized the concept of providing Quality Services by Medium & Large organizations.